scholarly journals Congenital hypofibrinogenemia: a case report

Author(s):  
Pandala Paramesh ◽  
Usha Rani Thota ◽  
Rakesh Kotha

Fibrinogen disorders are rare bleeding disorders. Fibrinogen is also called factor I which is involved in last step of coagulation cascade. Congenital hypofibrinogenemia is usually caused by mutation of FIB (fibrinogen-binding protein) gene. These disorders should be suspected when Thrombin time is prolonged in well look child with history of bleeding manifestations. We are describing a female child who is having pallor with history of recurrent ecchymosis and minor post traumatic bleeding. Based on coagulation screening profile, we made the diagnosis of hypofibrinogenemia.

2021 ◽  
Vol 8 (8) ◽  
pp. 2495
Author(s):  
Madhusoodan Gupta ◽  
Deepti Varshney

Post traumatic near total amputation of apex of tongue is a rare scenario but when happens it causes life threatening situation due to active intraoral bleeding and risk of aspiration especially in children. Tongue is a unique organ which has very rich blood supply and resides in intraoral cavity. Due to its rich blood supply profuse bleeding is commonly seen after the tongue injury. It helps in swallowing, speech, taste, mastication and airway protection. It facilitates perception of gustatory stimuli. Here author presents a case of 13 months old female child, who presented to emergency department with history of fell down from the bed and sustained tongue injury with profuse bleeding. On examination patient had near total amputation of apex of tongue. Gentle debridement followed by meticulous complex repair of intrinsic muscles of tongue was done. On post-operative day two patient was discharged uneventfully.


2013 ◽  
Vol 96 (5) ◽  
pp. 2857-2865 ◽  
Author(s):  
R. Sunagar ◽  
S.N. Deore ◽  
P.V. Deshpande ◽  
A. Rizwan ◽  
A.D. Sannejal ◽  
...  

2021 ◽  
Vol 15 (1) ◽  
Author(s):  
Charity Wiafe Akenten ◽  
Kennedy Gyau Boahen ◽  
Kwadwo Sarfo Marfo ◽  
Nimako Sarpong ◽  
Denise Dekker ◽  
...  

Abstract Background The increasing incidence of multi-antibiotic-resistant bacterial infections, coupled with the risk of co-infections in malaria-endemic regions, complicates accurate diagnosis and prolongs hospitalization, thereby increasing the total cost of illness. Further, there are challenges in making the correct choice of antibiotic treatment and duration, precipitated by a lack of access to microbial culture facilities in many hospitals in Ghana. The aim of this case report is to highlight the need for blood cultures or alternative rapid tests to be performed routinely in malaria patients, to diagnose co-infections with bacteria, especially when symptoms persist after antimalarial treatment. Case presentation A 6-month old black female child presented to the Agogo Presbyterian Hospital with fever, diarrhea, and a 3-day history of cough. A rapid diagnostic test for malaria and Malaria microscopy was positive for P. falciparum with a parasitemia of 224 parasites/μl. The patient was treated with Intravenous Artesunate, parental antibiotics (cefuroxime and gentamicin) and oral dispersible zinc tablets in addition to intravenous fluids. Blood culture yielded Acinetobacter baumanii, which was resistant to all of the third-generation antibiotics included in the susceptibility test conducted, but sensitive to ciprofloxacin and gentamicin. After augmenting treatment with intravenous ciprofloxacin, all symptoms resolved. Conclusion Even though this study cannot confirm whether the bacterial infection was nosocomial or otherwise, the case highlights the necessity to test malaria patients for possible co-infections, especially when fever persists after parasites have been cleared from the bloodstream. Bacterial blood cultures and antimicrobial susceptibility testing should be routinely performed to guide treatment options for febril illnesses in Ghana in order to reduce inappropriate use of broad-spectrum antibiotics and limit the development of antimicrobial resistance.


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